Dead wood volume to dead wood carbon: the issue of conversion factors

Requirements for emission reporting under the Kyoto protocol demand an estimate of the dead wood carbon pool in forests. The volume of dead wood consists of coarse woody debris, smaller woody debris and dead roots. The measurement of dead wood volume was included in the most recent National Forest Inventory in Switzerland. To convert dead wood volume into carbon two conversion factors are required: (a) carbon (C) concentration and (b) wood density. So far internationally accepted default values for C concentration (50%) and for wood density (density of alive trees) were used as default values to estimate dead wood carbon, since local measurements were lacking. However, in a field study at 34 sites in Switzerland, the C concentration and density of CWD from Picea abies and Fagus sylvatica of four decay classes were measured recently. The results showed that C concentration in CWD differed significantly between species but did not change due to decay class. The density of CWD decreased significantly with an increase in decay class and it also differed between species. The decrease in CWD density was more pronounced for F. sylvatica than for P. abies. We assessed correlations between climate attributes and CWD density using regression analysis. The modeled densities and measured C concentrations were then expanded with the help of CWD volume data from the NFI3. Spruce CWD and thus spruce CWD carbon is much more abundant in Swiss forests than beech CWD carbon. The majority of spruce CWD is located in the Alps and Pre-Alps. The CWD volume from P. abies was 10 times higher than that from F. sylvatica. Thus, changes in conversion factors for P. abies CWD affected the overall estimate of dead wood carbon in Swiss forests much more than changes in conversion factors for F. sylvatica CWD. Current improvements in CWD conversion factors decreased the estimated amount of spruce CWD carbon by 23.1% and that of beech by 47.6%. The estimated amount of CWD carbon in Swiss forests is decreased by 31%. Since improved estimation methods are currently not applied to smaller woody debris and dead root material, the estimated amount of dead wood carbon is only reduced by 15%. Improving conversion factors for all dead wood fractions would presumably decrease the amount of dead wood carbon by additional 16%.     

The effect of girdling on the moisture content of small-sized trees

In this study, the effect of girdling on the moisture content of small-sized trees for heat energy production was clarified. The moisture content was measured for Scots pine (Pinus sylvestris), Norway spruce (Picea abies), and Downy birch (Betula pubescens) during two growing seasons after girdling. The trees were girdled at breast height for around 30 cm by removing the bark, phloem, and cambium from around the stem. At the beginning of the growing season the mean moisture content of the living Scots pine (P. sylvestris) and Norway spruce (P. abies) was 60%, and for Downy birch (B. pubescens) it was 50%. During the first growing season the effect of girdling on the moisture content was low, but during the second growing season the moisture content decreased significantly. The moisture content of the Norway spruce (P. abies) (23%) and Downy birch (B. pubescens) (33%) was at its lowest point at 14 months after girdling. There were no significant changes in the moisture content of the Scots pine (P. sylvestris) in this study. The results of this study can be used in basic research and in the development of energy wood production.     

Infection experiments with Gremmeniella abietina on seedlings of Norway spruce and Scots pine

Conidia of Gremmeniella abietina infected and caused disease symptoms in annual shoots of both Scots pine (Pinus sylvestris) and Norway spruce (Picea abies) seedlings. In Norway spruce shoots the infection remained largely latent, with only a few seedlings showing symptoms. Mycelial growth inside the shoots was faster in Scots pine than in Norway spruce and was favoured by low temperature in both hosts. The shoots of Norway spruce seedlings had higher endophyte populations than those of Scots pine, and the populations were decreased by low temperatures. Reductions in the normal epiphytic or endophytic flora by acid mist treatments seemed to favour the development of G. abietina.     

Height growth of planted conifer seedlings in relation to solar radiation and position in Scots pine shelterwood

Seedlings of different provenances of Scots pine (Pinus sylvestris L.), lodgepole pine (Pinus contorta Dougl., var. latifolia Engelm.) and Norway spruce (Picea abies (L.) Karst.) were planted in three Scots pine shelterwoods (125, 65 and 43 stems ha⁻¹) and a clear-cut, all in northern Sweden. The sites were mounded and planting took place during 2 consecutive years (1988 and 1989). The solar radiation experienced by the individual seedlings was determined using a simulation model. Height development of the seedlings was examined during their first 6 years after planting. During the final 3 years of the study, height growth of Norway spruce was relatively poor, both in the shelterwoods and the clear-cut area. Height growth of lodgepole pine was significantly greater than that of Scots pine, both in the shelterwoods and the clear-cut. In contrast to Norway spruce, Scots pine and lodgepole pine displayed significantly greater height growth in the clear-cut than in the shelterwoods. For all three species in the shelterwoods, regression analyses showed that height growth was more strongly correlated with the distance to the nearest tree than with the amount of radiation reaching the ground, i.e. growth was reduced in the vicinity of shelter trees. Therefore, we conclude that the significant reduction in height growth of seedlings of Scots pine and lodgepole pine in Scots pine shelterwoods was partially caused by factors associated with the distance to the nearest shelter tree. Because the substrate was a nitrogen-poor sandy soil, we suggest that root competition for mineral nutrients, especially nitrogen, accounts for the reduction in height growth.     

Colour responses from wood,thermally modified in superheated steam and pressurized steam atmospheres

Abstract

In this study, two different methods were used to produce thermally modified wood. One was carried out in a typical kiln drying chamber using superheated steam (SS) and the other used pressurized steam in an autoclave cylinder (PS). Overall, both processes followed the same principles and the wood was not treated with any chemicals. Two wood species were studied, Scots pine (Pinus sylvestris) and Norway spruce (Picea abies). Treatments in the autoclave were carried out under pressure using temperatures of 160°C, 170°C and 180°C. Temperatures of 190°C and 212°C were used in treatments in the chamber at normal air pressure. The colour was measured using L*C*H colour space. Results for both species showed that similar L* (lightness) can be reached at lower (20–30°C) temperatures using PS compared with SS treatment. The hue angle of PS-treated wood was smaller than that of SS-treated wood. No significant difference in C* (chroma) was detected. The difference in E value between PS- and SS-treated wood was smaller for Norway spruce than for Scots pine. The residual moisture content was about 10% higher in wood treated by the PS process compared with the SS process.     

Superoxide dismutase (SOD) activity in Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies L. Karst.) needles in northern Finland

The superoxide dismutase (SOD EC 1.15.1.1) activity in Scots pine (Pinus sylvestris) and Norway spruce (Picea abies L. Karst.) needles in urban and rural trees of northern Finnish populations was studied. Enzyme activity was higher in pine than in spruce needles. Two pine clones from eastern Finland and Lapland revealed great differences in specific SOD enzyme activity.     

Equations for estimating above- and belowground biomass of Norway spruce,Scots pine,birch spp. and European aspen in Latvia

This study aims to derive allometric functions to estimate the above- and belowground biomass components of the most important tree species in Latvia. The study material included a total of 81 Norway spruce (Picea abies [L.] Karst), 102 Scots pine (Pinus sylvestris L.), 105 birch spp. (mainly silver birch (Betula pendula Roth)) and 84 European aspen (Populus tremula L.) trees sampled in 124 forest stands. The suitability of three mathematical models for the prediction of total aboveground biomass, stem biomass, total live and dead branch biomass, belowground biomass and small root biomass was evaluated. Our analysis revealed that the use of the Intergovernmental Panel on Climate Change mean default values for the root-to-shoot ratio recommended for temperate and boreal ecological zones leads to the overestimation of root biomass of young trees, especially Scots pine and Norway spruce. Our findings indicate that biomass functions recommended for other Baltic Sea countries are not appropriate for the assessment of the biomass stock in Latvia’s forests because these lead to biased estimates. The biomass functions derived in our study are recommended for reporting the biomass stock in Latvia.     

Seasonal dynamics of wood formation: a comparison between pinning,microcoring and dendrometer measurements

Three different methods were evaluated for analysing wood formation of Norway spruce [Picea abies (L.) Karst.] and Scots pine (Pinus sylvestris L.) in Finland. During two growing seasons, wood formation dynamics were determined both by wounding the cambium with a needle followed by localisation of the wound-associated tissue modification after the growing season (pinning), and by extracting small increment cores during the growing season (microcoring). Stem radius was additionally monitored with band dendrometers. For Norway spruce, pinning and microcoring yielded similar dates for the onset of wood formation. The timing of wood production during the growing season was also similar for pinning and microcoring. For Scots pine, the onset of wood formation was recorded from microcores almost 2 weeks later than from pinning samples. In Scots pine, microcore measurements also produced somewhat later cessation dates for tracheid formation than the pinning samples. For both tree species, the total number of tracheids formed during the growing season was, however, about the same for pinning and microcoring. Dendrometer results clearly differed from those of pinning and microcoring. In particular, the dendrometers showed an increase of stem radius considerably earlier in spring, when the other methods did not detect wood formation. Thus, pinning and microcoring currently represent the most reliable techniques for detailed monitoring of wood formation.     

Modelling dominant height growth from national forest inventory individual tree data with short time series and large age errors

We developed dominant height growth models for Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) in Norway using national forest inventory (NFI) data. The data were collected for a different purpose which potentially causes problems for dominant height growth modelling due to short time series and large age errors. We used the generalized algebraic difference approach and fitted 15 different models using nested regression techniques. Despite the potential problems of NFI data the models fitted to these data were unbiased for most of the age and site index range covered by the NFI data when tested against independent data from long-term experiments (LTE). Biased predictions for young stands and better site indices that are better represented in the LTE data, led us to fit models to a combined data set for unbiased predictions across the total data range. The models fitted to the combined data that were unbiased with little residual variation when tested against an independent data set based on stem analysis of 73 sample trees from southeastern Norway. No indications of regional differences in dominant height growth across Norway were detected. We tested whether the better growing conditions during the short time series (22 years) of the NFI data had affected our dominant height growth models relative to long-term growing conditions, but found only minor bias. The combination with LTE data that have been collected during a longer period (91 years) reduced this potential bias. The dominant height growth models presented here can be used as potential height growth models in individual tree-based forest growth models or as site index models.     

Compaction of till soils and growth tests with Norway spruce and scots pine

Five of the most common soils in forest areas in Sweden, viz., coarse sand, fine sand, coarse sandy till, medium sandy till and fine sandy till soil, were compressed at different loadings for 10 min. In the soils studied, it was found that the more fine material there was in the soil, the easier it compacted, and that till soils compacted much more than sediments of the same main particle class. The chosen compression time seemed to correspond well with an equilibrium level of static compaction. Influence of wall friction in compression tubes was found to be negligible for till soils.After compaction the soil cores were sown with Norway spruce (Picea abies (L.) Karst.) or Scots pine (Pinus sylvestris L.) and 16–20 days later the root lengths were recorded. Lengths of primary roots in per cent of the control were found to be almost inverse to the compaction of the soils; Norway spruce was more impeded than Scots pine. Thus, the bulk density alone is a poor indicator of the impact of soil compaction. Growth to 26, 33 and 120 days showed that the extension of secondary roots might be more impeded by compaction than the primary roots. Fertilization increased growth but did not decrease the growth difference between seedlings on unloaded and loaded soil cores.     

Freezing temperatures in the root zone—effects on growth of containerized Pinus sylvestris and Picea abies seedlings

Roots of 1‐year‐old containerized seedlings of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) were experimentally frozen in December. The seedlings were then grown for 3 weeks in a growth chamber and evaluated with regard to root growth capacity (RGC) and shoot elongation. The subsequent RGC of Scots pine declined as root zone temperatures were lowered from ‐6°C to ‐11°C and from ‐11°C to ‐16°C. Almost no root growth was observed after exposure to ‐20°C. Shoot growth was also negatively affected by low root temperatures but less than root growth. Low root temperatures did not affect Norway spruce as much as Scots pine, although root and shoot growth of Norway spruce were reduced after exposure to the lowest test temperatures (‐16°C and ‐20°C). The length of exposure, ranging between 1 and 8 hours had no effect on subsequent growth.     

A study of the structure of wood cells by x-ray diffraction

Summary An x-ray diffraction method was used to determine the values of the mean microfibrillar helical angles and to estimate quantitatively the amount of crystalline cellulose in the various cell wall layers of wood fibers. To interprete the intensity variation along the diffraction arcs a new curve fitting method based on Gaussian pairs was developed. As an application results are given for Scots pine (Pinus sylvestris) and Norway spruce (Picea abies).the authors acknowledge the financial support by the National Research Council for Science, Finland     

Growth response of coniferous stands to whole‐tree harvesting in early thinnings

A series of 15 field experiments was established to quantify the growth response of first‐thinning stands of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst) to whole‐tree harvesting and to estimate the need for nutrient compensation. The experiments were undertaken in Finland, Norway and Sweden and represent a wide range of site conditions. The site index (H ₁₀₀) of Scots pine stands varied from 19 to 29 m, and that of Norway spruce stands from 28 to 36 m. Total amounts of biomass and nutrients removed were calculated based on data obtained from felled sample trees. During the first 5‐yr period the growth response to the removal of logging residues varied considerably in both pine and spruce stands. Regression analyses did not reveal any functions that explained the variation in results satisfactorily. In cases where whole‐tree harvesting influenced tree growth negatively, this effect was counteracted by compensatory fertilization. It was concluded that to determine the response of remaining trees to harvesting intensity reliably, the post‐harvest period analysed must be longer than 5 yrs.     

Distribution of preservatives in thermally modified Scots pine and Norway spruce sapwood

Studying the impregnation and distribution of oil-based preservative in dried wood is complicated as wood is a nonhomogeneous, hygroscopic and porous material, and especially of anisotropic nature. However, this study is important since it has influence on the durability of wood. To enhance the durability of thermally modified wood, a new method for preservative impregnation is introduced, avoiding the need for external pressure or vacuum. This article presents a study on preservative distribution in thermally treated Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) sapwood using computed tomography scanning, light microscopy, and scanning electron microscopy. Secondary treatment of thermally modified wood was performed on a laboratory scale by impregnation with two types of preservatives, viz. Elit Träskydd (Beckers) and pine tar (tar), to evaluate their distribution in the wood cells. Preservative solutions were impregnated in the wood using a simple and effective method. Samples were preheated to 170 °C in a drying oven and immediately submerged in preservative solutions for simultaneous impregnation and cooling. Tar penetration was found higher than Beckers, and their distribution decreased with increasing sample length. Owing to some anatomical properties, uptake of preservatives was low in spruce. Besides, dry-induced interstitial spaces, which are proven important flow paths for seasoned wood, were not observed in this species.     

Root growth capacity and field performance of Pinus sylvestris and Picea abies seedlings

Correlations between root growth capacity (RGC), at the time of planting, and field performance were studied for Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) seedlings. Before planting a gradient in seedling viability was generated through exposure to low root temperatures and different winter storage regimes. The hypothesis that high RGC values would improve field performance was to some extent verified for pine seedlings while no correlations could be registered for spruce. Reasons for these results are discussed.     

Heterobasidion annosum root rot in Picea abies: Modelling economic outcomes of stump treatment in Scandinavian coniferous forests

Abstract

The economic outcomes of stump treatment against spore infections of the root rot pathogen Heterobasiodion annosum s. l. were analysed based on simulations in four stands typical of Swedish forestry and forest management: (A) Norway spruce [Picea abies (L.) Karst.] stand on former agricultural soil (SI?=?32), (B) Norway spruce stand (SI?=?26) on forest land; (C) Mixed stand of Norway spruce and Scots pine (Pinus sylvestris L.) (SI?=?24) with only H. parviporum present, i.e. no infection of Scots pine and no possibility of interspecies spread of disease between hosts; and (D) same as C, but H. annosum s. str. (Fr.) Bref and H. parviporum Niemelä & Korhonen present, i.e. interspecies spread of disease possible. Models for disease development, growth and yield and cross-cutting were used in the simulations. The simulated decay frequency in Norway spruce trees ranged between 2 and 90%. Stump treatment at the previous final felling and in all thinning operations was profitable at interest rates 1 and 3% in stands A, B and D, but not in stand C. In stand C, no stump treatment at all or treatment in thinnings only gave the highest net future value. Implications for stump treatment in practical forestry are discussed.     

Growth in supplementarily planted Picea abies regenerations

Abstract

An experiment was established in 1978 in two Norway spruce [Picea abies (L.) Karst.] plantations in southern Sweden to study yield after mortality in patches with and without supplementarily planted (SP) seedlings. Gaps of different sizes were created by removing the originally planted seedlings. The gaps were either left unplanted or a supplementary planting was performed with one of four species [Norway spruce, Scots pine (Pinus sylvestris L.), lodgepole pine (Pinus contorta Dougl.) or hybrid larch (Larix deciduas Mill×L. Leptolepis Gord.)] 2 (at Knäred) or 6 years (at Ullasjö) after the original plantation. In 2002, most of the SP Scots pine, lodgepole pine and hybrid larch seedlings were dead or severely damaged by roe deer and moose. Survival was high among SP Norway spruces, but they had slower growth than the originally planted spruces. Growth was lower at Ullasjö than at Knäred. In Ullasjö, growth was lower in small gaps than in large gaps. Trees in original regeneration in areas surrounding unplanted gaps were larger than trees surrounding gaps with SP seedlings, which in turn were larger than originally planted trees in plots without gaps. In conclusion, because the original plantation surrounding unplanted gaps used a large part of the open space and growth of SP seedlings was slow, supplementary planting resulted in an insignificant growth increase. However, supplementary planting may increase the timber quality of trees surrounding the gaps, although this effect remains to be quantified.     

Intraspecific variation in Heterobasidion annosum for growth in sapwood of Picea abies and Pinus sylvestris

Two greenhouse experiments were conducted to study intraspecific variation in growth of the root rot fungus Heterobasidion annosum in living host sapwood. In experiment 1, Scots pine (Pinus sylvestris) and Norway spruce (Picea abies) seedlings were inoculated with H. annosum isolates, 14 each of the S-and P-intersterility groups, collected from various parts of Sweden. In pine, the P-group isolates were more virulent than the S-group isolates both in terms of infection frequency, induced mortality rate (p < 0.05), and fungal growth in sapwood (p < 0.05). In spruce, the P-group isolates were also more virulent on average, but the difference was not statistically significant. Both S and P isolates had a higher infection frequency and a significantly longer sapwood growth on spruce than on pine. The P-group caused higher mortality on pine than on spruce. The length of the lesion in the inner bark was strongly correlated with fungal growth in spruce, but not in pine where the lesions were short or absent. In experiment 2, ten Norway spruce clones were inoculated with 18 S-isolates, originating from nine live-decayed trees and from nine spore-infected stumps in a single Norway spruce stand. The objective was to test whether any selection for growth rate in sapwood was detectable among individuals of H. annosum originating either from stumps or trees. The results gave no support for such selection since no difference in sapwood growth between the two groups of isolates was found.     

Carbon and nitrogen release from decomposing Scots pine,Norway spruce and silver birch stumps

Stumps are the largest coarse woody debris component in managed forests, but their role in nutrient cycling is poorly understood. We studied carbon (C) and nitrogen (N) dynamics in Scots pine (Pinus sylvestris), Norway spruce (Picea abies), and silver birch (Betula pendula) stumps, which had decomposed for 0, 5, 10, 20, 30 and 40 years after clear-cutting in southern Finland. Carbon and N were released significantly faster from birch stumps than from conifer stumps. In 40 years, conifer stumps lost 78% and birch stumps 90% of their initial C. In contrast, the amount of N in stumps increased, indicating that external N accumulated in the stumps. After 40 years of decomposition, the amount of N was 1.7 and 2.7 times higher than the initial amount in pine and spruce stumps, respectively. Nitrogen was released from birch stumps, but only after they had decomposed for 20 or more years. On average, 59% of N stored in birch stumps was released during 40 years. The results indicate that the stumps of the major tree species in Fennoscandian forests are long-term C and, especially, N pools which serve as N sinks, thus potentially diminishing N leaching into ground water and watercourses after harvesting. This suggests that the removal of stumps for bioenergy production may markedly affect the nutrient status and nutrient cycling of boreal forests.     

Effect of uninucleate Rhizoctonia on Scots pine and Norway spruce seedlings

One‐year‐old container‐grown seedlings were planted in spring on clear cut areas: the Norway spruce (Picea abies) on a moist upland site (Myrtillus‐type) and Scots pine (Pinus sylvestris) on a dryish upland site (Vaccinium‐type). While still in the nursery, half of the seedlings of each species had been inoculated during the previous summer, with a uninucleate Rhizoctonia sp., a root dieback fungus. At outplanting all the seedlings appeared healthy and had a normal apical bud, although the height of the inoculated seedlings was less than that of the uninoculated control seedlings. At the end of the first growing season after planting, the mortality of inoculated Scots pine and Norway spruce seedlings was 25 and 69%, respectively. After two growing seasons the mortality of inoculated seedlings had increased to 38% for Scots pine and 93% for Norway spruce. The mortality of control seedlings after two growing seasons in the forest was 2% for Scots pine and 13% for Norway spruce. After outplanting the annual growth of inoculated seedlings was poor compared with the growth of control seedlings. These results show that, although Rhizoctonia‐affected seedlings are alive and green in the nursery, the disease subsequently affects both their survival and growth in the forest.